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Four novel p.N385K, p.V36A, c.1033-1034insT and c.1417-1418delCT mutations in the sphingomyelin Phosphodiesterase 1 (SMPD1) gene in patients with types A and B Niemann-Pick disease (NPD).
Manshadi MD, Kamalidehghan B, Keshavarzi F, Aryani O, Dadgar S, Arastehkani A, Tondar M, Ahmadipour F, Meng GY, Houshmand M. Manshadi MD, et al. Among authors: ahmadipour f. Int J Mol Sci. 2015 Mar 24;16(4):6668-76. doi: 10.3390/ijms16046668. Int J Mol Sci. 2015. PMID: 25811928 Free PMC article.
Four novel ARSA gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations.
Dehghan Manshadi M, Kamalidehghan B, Aryani O, Khalili E, Dadgar S, Tondar M, Ahmadipour F, Yong Meng G, Houshmand M. Dehghan Manshadi M, et al. Among authors: ahmadipour f. Ther Clin Risk Manag. 2017 Jun 16;13:725-731. doi: 10.2147/TCRM.S119967. eCollection 2017. Ther Clin Risk Manag. 2017. PMID: 28670130 Free PMC article.
Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss.
Balali M, Kamalidehghan B, Farhadi M, Ahmadipour F, Ashkezari MD, Hemami MR, Arabzadeh H, Falah M, Meng GY, Houshmand M. Balali M, et al. Among authors: ahmadipour f. Ther Clin Risk Manag. 2016 Jan 28;12:117-28. doi: 10.2147/TCRM.S90581. eCollection 2016. Ther Clin Risk Manag. 2016. PMID: 26889084 Free PMC article.
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